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Clinical Trials/NCT05277519
NCT05277519RecruitingNot Applicable

Neuroplasticity Induced by Functional Muscle Tendon Vibrations in Patients With Acquired Brain Injury

Institut National de la Santé Et de la Recherche Médicale, France1 site in 1 country56 target enrollmentStarted: June 16, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
56
Locations
1
Primary Endpoint
Baseline EMG

Study Overview

Brief Summary

Sequences of muscle tendon vibrations allow to reproduce the sensory feedback during movement like locomotion and kinaesthesia. It is known that such a treatment promotes motor recovery after stroke assuming that it enhances neuroplasticity. The aim of the research is to study the activity in cerebrospinal circuitry to evaluate the neuroplastic changes during and after instrumented proprioceptive rehabilitation relying on sequences of muscle vibration in subacute stroke stages.

Detailed Description

Randomized control trial : 28 patients with active vibrations vs. 28 patients with sham stimulation Subacute phase : D15 to 6 months after stroke or patients with traumatic brain injury with similar semiology as stroke (hemiparesis) Measure at baseline : Electrophysiological investigations (EMG,EEG, MRI, clinical evaluation) Treatment of 5 weeks with 3 sessions of vibrations or sham a week Evaluation at mid time (electrophysiology and clinical examinations) Final examination (electrophysiology, MRI and clinical examination)

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •hemiparesis at least transient in lower limb following an acquired brain injury (stroke or traumatic brain injury)
  • •French spoken
  • •Affiliated to a French social insurance
  • •No previous traumatic, vascular or neurodegenerative injuries
  • •Having presented during the acute phase or presenting a motor deficit of one of the lower limbs
  • •Presenting an absence of autonomy of walking at the entrance of the rehabilitation department
  • •In the sub-acute phase, i.e. from 15 days to 6 months after the accident
  • •Presenting moderate cognitive disorders allowing them to understand instructions and give their consent

Exclusion Criteria

  • •strong cognitive disorders
  • •maintenance of justice, tutelage, legal guardianship
  • •Pregnancy and breastfeeding
  • •Outpatients who do not have weekly follow-up in the rehabilitation department

Outcomes

Primary Outcomes

Baseline EMG

Time Frame: Evaluation at baseline (4 days before treatment)

H-reflex and reciprocal inhibition

EMG change from baseline after 2-week treatment

Time Frame: Evaluation during the 3rd week of treatment

H-reflex and reciprocal inhibition

EEG change from baseline after 2-week treatment

Time Frame: Evaluation during the 3rd week of treatment

SEP and resting state activity

EMG change after the 5-week treatment

Time Frame: Evaluation 4 days after the end of the 5-week treatment

H-reflex and reciprocal inhibition

Baseline EEG

Time Frame: Evaluation at baseline (4 days before treatment)

SEP and resting state activity

EEG change after the 5-week treatment

Time Frame: Evaluation 4 days after the end of the 5-week treatment

SEP and resting state activity

Secondary Outcomes

  • Baseline Muscle Strength(Evaluation at baseline (4 days before treatment))
  • Walking from baseline after 5-week treatment(Evaluation 4 days after the end of the 5-week treatment)
  • Change in MD(Evaluation 4 days after the end of the 5-week treatment)
  • Sensorimotor function change from baseline after 5-week treatment(Evaluation 4 days after the end of the 5-week treatment)
  • Spasticity change from baseline after 2-week treatment(Evaluation during the 3rd week of treatment)
  • Baseline Balance(Evaluation at baseline (4 days before treatment))
  • Baseline walking(Evaluation at baseline (4 days before treatment))
  • Change in FA(Evaluation 4 days after the end of the 5-week treatment)
  • Baseline MD(Evaluation at baseline (4 days before treatment))
  • Baseline FA(Evaluation at baseline (4 days before treatment))
  • Muscle Strength change from baseline after 2-week treatment(Evaluation during the 3rd week of treatment)
  • Muscle Strength change from baseline after 5-week treatment(Evaluation 4 days after the end of the 5-week treatment)
  • Baseline Spasticity(Evaluation at baseline (4 days before treatment))
  • Spasticity change from baseline after 5-week treatment(Evaluation 4 days after the end of the 5-week treatment)
  • Baseline sensorimotor function(Evaluation at baseline (4 days before treatment))
  • Sensorimotor function change from baseline after 2-week treatment(Evaluation during the 3rd week of treatment)
  • Balance change from baseline after 2-week treatment(Evaluation during the 3rd week of treatment)
  • Balance change from baseline after 5-week treatment(Evaluation 4 days after the end of the 5-week treatment)
  • Walking from baseline after 2-week treatment(Evaluation during the 3rd week of treatment)

Investigators

Sponsor
Institut National de la Santé Et de la Recherche Médicale, France
Sponsor Class
Other Gov
Responsible Party
Sponsor

Study Sites (1)

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